US 7027163 B2
A fast, accurate and reliable sensor applicable to chemical and biological analytes resides in an optical grating-based sensor, sensing system, and method of use. The sensor, configured for use with an illumination source and a signal detector in the system embodiment, includes first and second periodic diffraction gratings superimposed and shifted laterally relative to each other by a distance of less than one period, such that the illumination from the source is affected by both gratings before reaching the detector. An analyte recognition material disposed on a surface of the second diffraction grating. In operation, the output of the detector is first used to establish a baseline optical phase signal. The analyte recognition material is exposed to a sample, and the output of the detector is used to to determine a second optical phase signal. The baseline optical phase signal is compared to the second optical phase signal to detect the presence of the analyte, if any, in the sample. The analyte recognition material may be an antibody, nucleic acid, lectin or other substance. The sample may obtained from a mammal, including a human, plant, or the environment.
1. An optical sensor comprising:
a first periodic diffraction grating;
a second periodic diffraction grating, the gratings being superimposed and shifted laterally relative to each other by a distance of less than one period;
an analyte recognition material disposed on a surface of the second diffraction grating;
an illumination source directing illumination onto the first grating; and
a detector disposed relative to the second grating such that illumination passing through the second grating reaches the detector.
2. The optical sensor of
3. The optical sensor of
4. The optical sensor of
5. The optical sensor of
6. The optical sensor of
7. The optical sensor of
8. A method of detecting an analyte, comprising the steps of:
providing the optical sensor of
sampling the output of the detector to establish a baseline optical phase signal;
exposing the analyte recognition material to the sample;
sampling the output of the detector to determine a second optical phase signal; and comparing the baseline optical phase signal to the second optical phase signal to detect the presence of the analyte, if any in the sample.
9. The method of
10. The method of
11. The method of
12. The method of
13. The method of
14. The method of
15. The method of
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17. The method of
18. The method of
19. An optical sensor configured for use with an illumination source and a signal detector, comprising:
a first periodic diffraction grating;
a second periodic diffraction grating, the gratings being superimposed and shifted laterally relative to each other by a distance of less than one period such that the illumination from the source is affected by both gratings before reaching the detector; and
an analyte recognition material disposed on the surface of the second diffraction grating.
20. The optical sensor of
21. The optical sensor of
22. The optical sensor of
23. The optical sensor of
24. The optical sensor of
25. The method of
This invention relates to sensor devices for detecting chemical and biological agents. In particular, the invention relates to chemical and biological agent sensor devices that detect phase changes in light incident on two diffraction gratings.
Biological weapons, infectious diseases, and environmental pathogens threaten both military and civilian personnel. Current technology lacks the capability to accurately detect the presence of trace amounts of chemical and biological warfare agents quickly and reliably.
Current technologies include those involving detection of analytes labeled with a fluorescent, photo-luminescent, radioactive or enzymatic marker. This requirement includes additional steps and expense to the detection process, a significant disadvantage when prompt detection is necessary.
Another broad category of currently used sensors includes those that employ optical waveguides. Waveguide sensors typically have the disadvantages of high sensitivity to changes in the ambient conditions such as temperature, resulting in undesirable signal to noise ratios.
Other known sensors monitor changes in the intensity of several diffraction orders to detect the occurrence of a biological binding event. However, intensity (irradiance) measurements are not sensitive enough for many applications and are sensitive to noise, resulting in difficulty in relating and quantifying the changes in the detected diffraction irradiance signal to an input stimulus.
This invention improves upon the existing art by proving a fast, accurate and reliable sensor applicable to chemical and biological analytes. The invention covers an optical grating-based sensor, sensing system, and method of use. The sensor, configured for use with an illumination source and a signal detector in the system embodiment, includes first and second periodic diffraction gratings superimposed and shifted laterally relative to each other by a distance of less than one period, such that the illumination from the source is affected by both gratings before reaching the detector. An analyte recognition material disposed on a surface of the second diffraction grating.
Given this arrangement with the illumination source activated, the output of the detector is first used to establish a baseline optical phase signal. The analyte recognition material is exposed to a sample, and the output of the detector is used to determine a second optical phase signal. The baseline optical phase signal is compared to the second optical phase signal to detect the presence of the analyte, if any, in the sample.
The analyte recognition material may be an antibody, nucleic acid, lectin or other substance. The sample may be obtained from a mammal, including a human, plant, or the environment. A positioning system may be provided for moving one or both of the first and second gratings, and the system may further comprise a spatial filter disposed relative to the second grating such that selected orders of diffracted light are prevented from reaching the detector.
A grating sensor according to the present invention is a photonic device that includes an optical grating structure having at least two individual gratings. The two gratings, each having a periodic structure, are positioned parallel to each other, such that the periodic structure are superimposed and shifted laterally relative to each other. This lateral shift is less than one period and is preferably a shift of one quarter period. Further, at least one of the gratings includes an analyte recognition material operable to interact specifically with an analyte of interest. A change in the depth of modulation in one of the gratings caused by specific interaction of an analyte with an analyte recognition material results in a change in optical phase. The phase change is sensed by a detector and output as signal. The grating sensor may further include a translation device adapted to move one or more of the gratings in order to modulate the signal.
Gratings suitable for use in an inventive sensor and methods of their generation are known in the art. A grating is selected for a particular sensor application according to characteristics and properties required, which will be recognized by one of skill in the art. Characteristics and modifiable properties of individual gratings and their uses are set forth in references such as Hutley M. et al.; Diffraction Gratings; Academic Press; 1997 and E. Popov, et al., Diffraction Gratings and Applications; Marcel Dekker, Inc.; 1997. Modifiable grating parameters illustratively include period, index of refraction and modulation depth. The period of the grating determines the scatter angle of the diffracted orders; the peak-to-valley depth of the phase (i.e. refractive index) profile determines the amount of light that is diffracted into each order; and the lateral position of the grating determines the phase of the wavefront in each of the diffracted orders relative to the zero order. Further modifiable grating parameters include material composition of the grating, grating surface chemistry and type of analyte recognition material used, as described below.
An illustrative grating suitable for use in a sensor according to the present invention is described in Example 1 below.
A grating suitable for use in an inventive sensor includes a substrate material. The substrate material is a solid or firm gel illustratively including glass, silicon, metals such as aluminum, copper, gold, platinum titanium, alloys thereof, graphite, mica, and various polymers, such as polystyrene; polycarbonate; polymethylmethacrylate; polyvinylethylene; polyethyleneimine; polyoxymethylene; polyvinylphenol; polylactides; polymethacrylimide; polyalkenesulfone; polyhydroxyethylmethacrylate; polyvinylidenedifluoride; polydimethylsiloxane; polytetrafluorethylene; polyacrylamide; polyimide and block-copolymers. Choice of grating material depends on a number of factors such as the analyte sought to be detected, the analyte recognition material to be used and the surface chemistry suitable for immobilizing the analyte recognition material on the grating. Bowtell et al., DNA Microarrays: A Molecular Cloning Manual, Cold Spring Harbor Laboratory; 2002.
Grating Surface Chemistry
The substrate material of a grating used in an inventive sensor may have a modified surface for immobilizing an analyte recognition material by chemical bonding or adsorption. Surface modification, such as by chemical treatment of a surface to provide binding sites for an analyte recognition material depends on the particular analyte recognition material to be attached to the substrate and the composition of substrate. Modification of grating surface chemistry in order to attach an analyte recognition material is well known in the art and includes such illustrative methods as modification of silicon or silicon oxide surfaces with organo-functionalized silanes. such as alkoxy- and chloro-silanes. Further suitable silanes are listed in Silicon Compounds: Register & Review, from United Chemical Technologies, 5th Ed., 1991. In addition, many other surface chemistries and methods of modifying a grating substrate for binding an analyte recognition material are known, such as those commonly used to fabricate microarrays of proteins, nucleic acids and other materials. See, for example, M. Schena, et al., “Quantitative Monitoring of Gene Expression Patterns with a Complementary DNA Microarray”, Science, 270: 467–470, 1995; Hermanson et al., in Immobilized Affinity Ligand Techniques, Academic Press, Inc., 1992 and U.S. Pat. Nos. 6,479,301, 6,475,809, 6,444,318 and 6,410,229.
Advantageously, attachment of an analyte recognition material may be reversible such that the sensing surface of the grating is reusable.
Analyte Recognition Materials
An analyte recognition material is included on at least one of the gratings used in a sensor of the invention. As used herein, the term “analyte recognition material” is intended to mean a molecule that specifically binds to an entity to be detected, an analyte.
Analytes detected by a grating sensor according to the invention illustratively include an antibody, an antigen, a hapten, a receptor, a receptor ligand such as an agonist or antagonist, a lectin, a protein, a peptide, a polysaccharide, a toxin, a virus, a bacterium, a cell, a cell component such as an organelle, a particle such as a liposome or niosome, a nucleic acid, a drug and a prion. An analyte may be a fragment or metabolite of the substances listed above capable of specific interaction with an analyte recognition material. Nucleic acids illustratively include DNA, RNA, oligomers and aptamers. An analyte may also be a gas, illustratively including NO, O2 and CO2.
Exemplary analyte recognition materials immobilized on a grating of the inventive sensor include an antigen, antibody, hapten, carbohydrate, lectin, receptor, ligand, binding protein, toxin, substrate, enzyme and nucleic acid.
Specific interactions between an analyte and an analyte recognition material are well known in the art, as are reaction conditions under which specific interactions occur. Interactions an analyte and an analyte recognition material illustratively include those of the following types: antigen-antibody, carbohydrate-lectin, receptor-ligand, binding protein-toxin, substrate-enzyme, effector-enzyme, inhibitor-enzyme, nucleic acid pairing, binding protein-vitamin, binding protein-nucleic acid, reactive dye-protein, and reactive dye-nucleic acid. Reactions conditions include variables such as temperature, salt concentrations, pH and reaction time are known to affect binding and one of skill in the art will recognize the appropriate binding conditions for a particular analyte/analyte recognition material pair. Specific conditions are set forth in common references such as, for example, Bowtell et al., DNA Microarrays: A Molecular Cloning Manual, Cold Spring Harbor Laboratory; 2002; Sambrook et al., Molecular Cloning: A Laboratory Manual, Cold Spring Harbor Laboratory; 3rd edition, 2001; and Harlow et al., Using Antibodies: A Laboratory Manual: Portable Protocol No. I, Cold Spring Harbor Laboratory; 1998.
Deposition of Analyte Recognition Material on Grating Surface
Creating structured arrays of analyte recognition materials requires immobilization of those materials at discrete locations on the surface of a grating used in an inventive sensor. Deposition and patterning of an analyte recognition material on a grating is known in the prior art. Exemplary techniques used include photoresist technology, self-assembled monolayer deposition and photochemical techniques. Deposition and patterning are particularly important as a variable contributing to the refractive index of a particular grating. Adjustment of the refractive index of a grating may be one method of modulating the sensitivity of the grating sensor.
An exemplary method of analyte recognition material deposition and patterning is micro-contact printing, which is a type of soft lithography that transfers molecules onto substrates at specific locations with the use of a polymeric stamp that has been cast from a desired pattern or mold. This procedure is an established microfabrication technique for patterning chemicals, proteins, DNA, lipid membranes, and cells. A polymer stamp, typically a material such as poly dimethyl siloxane, has the analyte recognition material to be patterned adsorbed to it, rinsed and dried, and then placed into contact with a solid substrate. After some determined time, seconds to minutes, the stamp is removed and the substrate surface is left with a coating of the transferred analyte recognition material in the desired pattern.
Photolithographic techniques are also well known as a method to manufacture a photoresist material in a desired pattern. In this technique, a patterned photoresist masks regions of the substrate that are to be functionalized with an analyte recognition material and allow the placement of surface pacifying molecules. Once the photoresist is removed there will be rows of molecular functional groups, primed for further chemical attachment to an analyte recognition material, such as an antibody, patterned between rows of nonreactive, protein resistant surface bound species. A photolithographic process can potentially move the surface chemistry methodology is advantageous in larger scale manufacturability and greater reproducibility.
A further patterning method includes a photochemical method. For example, a silane monolayer may be chemisorbed onto the surface of an etched grating wafer. The silane is chosen to have a reactive functional group (e.g., thiol, amine) available for further reaction. Specific bifunctional linkers are chosen that contain a photoactive functional group at one end. These linkers will be covalently attached to the silane film such that the photoactive group is available for further reaction/modification. The substrates may then be positioned into the optical assembly, and light from a UV laser source used to create an interference pattern on the substrate that matches the etched grating groove period. This will produce surface patterned lines of active and nonactive functional groups. The active silane functional groups are then linked to an analyte recognition material, such as an IgG antibody. The linker molecules used in such a method is chosen depending on the analyte recognition material to be attached and the light to be used in patterning. A variety of photoactive bifunctional linkers is commercially available of which many are reactive towards UV light of ˜230–350 nm.
Further exemplary methods of analyte recognition material deposition and binding to a grating surface are detailed in references 3–5 and 8–11.
Following deposition of a surface chemistry component, such as a linker or an analyte recognition material, various techniques, such as ellipsometry, and atomic force microscopy (AFM) may be used to evaluate the deposition for artifacts and/or appropriate quantity and pattern.
Although the individual grating is discussed above as incorporating a single type of analyte recognition material, it will be recognized that a grating may incorporate more than one type of analyte recognition material in order to allow multiple analyte detection on single grating surface. In another embodiment, a grating structure can be configured to detect multiple analytes by overlaying multiple gratings in a single grating structure, much like a volume hologram, with each grating tailored to a specific analyte. In this case, differentiating between grating signals is achieved by utilizing different grating periods or by using several wavelengths.
Prevention of nonspecific binding of analytes and/or analyte recognition materials to a grating used in an inventive sensor is important in achieving an optimal signal to noise ratio. A number of different approaches have been used to reduce nonspecific binding to various surfaces. The adsorption of innocuous proteins such as bovine serum albumin (BSA) and casein has been used to block other proteins from binding during surface immobilization of antibodies. The attachment of poly (ethylene glycol) (PEG) groups to glass and metals has been an effective method of creating protein-resistant surfaces. Detergents, in particular non-ionic types such as the Tween and Triton series of surfactants and zwitterionic surfactants, have been used create “wetter” surfaces that inhibit protein surface adsorption.
Relative Position of Individual Gratings
The grating structure included in the grating sensor includes two individual gratings as described above. The individual gratings are variably configured with respect to each other dependant on factors such as grating geometry, diffraction order selection, wavelength of the light source used and the distance between the gratings.
As mentioned above, the two gratings, each having a periodic structure, are positioned parallel to each other, such that the periodic slits are superimposed and shifted laterally relative to each other. This lateral shift is less than one period and is preferably a shift of one quarter period. This arrangement is shown in
In one embodiment, as shown in
In an alternative embodiment, shown in
In the transverse dimension, the gratings are disposed with a minimum distance between them that allows fluid flow, typically greater than 1 nm. The maximal distance between gratings is defined by the width of the incident beam, the period of the grating, the wavelength, and the order of diffraction detected. In general, if the two gratings lie within the Rayleigh range or depth of focus of the incident beam, the minimum distance requirement is satisfied.
Multiple Agent Detection
More than one analyte may be detected using multiple analyte recognition materials and multiple gratings as illustrated in
Any wavelength of light which is not significantly absorbed by either the grating or the solution may be used for illumination in a sensor of the invention. Typically, a single wavelength is used, for example, 633 nm emitted by a He—Ne laser. In some multiple analyte detection systems according to the present invention, multiple wavelengths are used, each detecting a separate analyte as described below and as shown in
The grating structure is illuminated by two collimated beams, each at a specific angle, to achieve the interference between the desired first orders. The diffraction angle for a given period is wavelength dependent (see grating equation). Beam diameter is somewhat flexible. At the low end, the beam should at least cover at least two periods, but the diameter is small and the Raleigh range is short. At the high end, a large-diameter beam requires real estate and sufficient coverage in conjunction with the fabrication technique. Accordingly, the optimum is somewhere between the low and high ends.
A detector to be used in a sensor according to the invention is known in the art and includes such devices as oscilloscopes, digital cameras, CCD cameras and the like. The detection scheme is, for example, a derivative of a lithographic overlay alignment method, currently used in lithographic projection systems, which can detect lateral shifts of semiconductor wafer features down to the 10 nm range. Such detectors are described in, for example, U.S. Pat. Nos. 5,559,601 and 5,477,057.
A detector array may be used, for example, when multiple analytes are detected as shown in
Phase measurement is a very mature technology, such as is known in the field of commercial interferometry, and has inherent advantages over intensity measurements with regard to noise sources. Methods and devices for phase measurement are well known and commercially available.
A grating sensor according to the invention optionally includes a positioning system to dither the translation motion of the grating structure so as to modulate the baseline signal. Such positioning systems are known in the art and include piezo actuators such as piezoelectric transducers (pzt) commercially available and art recognized equivalents.
In another embodiment, a translation device with no moving parts is used, employing acoustically induced optical grating, for example.
Grating Sensor Theory of Detection
Information on grating sensor operation is as follows: given two electromagnetic waves of the form:
In the grating sensor device a sinusoidal phase grating is used and can be defined by the transmission function:
where: m is the peak to peak excursion of phase delay (depth modulation), f is the grating frequency, ψ, is the lateral ‘shift’ of the grating, rect is rectangular shaped aperture function with width l.
The far-field diffraction pattern when the transmission function of equation (3) is illuminated by a normally incident monochromatic plane wave is given by:
From (4), it can be seen that the introduction of the phase grating has deflected energy out of the zero order into a multitude of higher order components. The intensity of these orders is dependent on Jq(m/2) and phase of the orders is dependent on ψ, i.e. the shift, of the gratings as given by eiqψ.
Where the system is set up such that the +1 and −1 orders are made to coincide so as to generate a two beam interference condition as in equation (2), one beam would have an electric field of E+1∝eiψ while the second would have E−1∝e−iψ. Equation (2) becomes:
Measurement of phase to yield the lateral shift of a grating can be very precise and relates to changes in the depth of modulation. Depth of modulation can be converted to a lateral shift in position of a grating by placing two gratings adjacent to each other with one shifted by a ¼ grating period. Using some trigonometric relationships, it can be shown that:
Commercial interferometry systems are available whose minimum detectable limits are in the 1/1000 of a phase cycle. From
Grating Sensor in Operation
Steps of a method according to the invention for using the inventive grating sensor include a preliminary illumination of the grating structure before exposure to the sample or analyte in order to establish a baseline optical phase signal.
In an optional step of the inventive method, the grating structure is treated to inhibit non-specific binding of analyte to analyte recognition material. Typically, the grating is exposed to a surfactant, such as a dilute solution of TWEEN-20. Alternatively, a protein known not to specifically bind to the analyte recognition material is use, such as bovine serum albumin or the like. Following treatment for non-specific binding, the grating may be rinsed to remove any excess.
In a further step of the inventive method, a grating having an analyte recognition material is exposed to a sample putatively containing an analyte known to bind to the analyte recognition material disposed on the grating. The sample is exposed to the grating under conditions that will allow binding of the analyte to the analyte recognition material. Binding conditions for specific analyte/analyte recognition materials are known in the art. Variables such as temperature, salt concentrations, pH and reaction time are known to affect binding and one of skill in the art will recognize the appropriate binding conditions for a particular analyte/analyte recognition material pair. Specific conditions are set forth in common references such as, for example, Bowtell et al., DNA Microarrays: A Molecular Cloning Manual, Cold Spring Harbor Laboratory; 2002; Sambrook et al., Molecular Cloning: A Laboratory Manual, Cold Spring Harbor Laboratory; 3rd edition, 2001; and Harlow et al., Using Antibodies: A Laboratory Manual: Portable Protocol NO. I, Cold Spring Harbor Laboratory; 1998.
A sample may be a biological or chemical sample, such as a sample obtained from a human or other animal or from an environmental site where the earth, water or air are to be tested. A sample illustratively refers to a cells, tissue or physiological fluid, such as amniotic fluid, blood, cerebrospinal fluid, plasma, serum, saliva, semen, and other bodily fluids. A sample also includes fluid or a suspension of solids obtained from mucous membranes, wounds, tumors and organs. Further, a sample may be obtained to test for environmental contamination. For example, a surface, such as an air filter, suspected to be contaminated may be swabbed and the material obtained may be suspended in a solution for exposure to a grating.
Advantageously, neither the analyte nor the analyte recognition material is required to be labeled in a method according to the present invention. This allows faster processing of samples, while affording highly sensitive detection of analyte.
The exposure of the grating to the sample may be achieved in situ, that is, with the grating in place in the grating structure. For example, the sample may be introduced into the space between the two gratings.
Exposure of the grating to the sample may also be accomplished with the grating removed from the grating structure. For example, the sample may be applied to the grating, or the grating may be immersed in the sample, for the time required by the binding reaction. Subsequently, the grating may be placed in the grating structure.
Optionally, the grating is rinsed following exposure to the sample in order to remove excess sample and to stop the binding reaction.
Following exposure of the grating to the analyte, the grating structure is illuminated and the optical phase signal detected. Any change in the optical phase signal may be quantitated by comparison to the optical phase signal detected during the preliminary illumination step.
Optionally, the amount of analyte present in the sample is calculated as described above.
Multiple Analyte Detection—
Several detection configurations for multiple analyte detection are depicted in
The layout shown in
Interferograms recorded using a digital camera, a wavelength of 633 nm and optical glass gratings without an analyte recognition material are shown in
Any patents or publications mentioned in this specification are indicative of the levels of those skilled in the art to which the invention pertains. These patents and publications are herein incorporated by reference to the same extent as if each individual publication was specifically and individually indicated to be incorporated by reference.
One skilled in the art will readily appreciate that the present invention is well adapted to carry out the objects and obtain the ends and advantages mentioned, as well as those inherent therein. The present methods, procedures, treatments, molecules, and specific compounds described herein are presently representative of preferred embodiments, are exemplary, and are not intended as limitations on the scope of the invention. Changes therein and other uses will occur to those skilled in the art which are encompassed within the spirit of the invention as defined by the scope of the claims.
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